Clinical Data Services

Our vast experience in clinical data services helps us understand the nuances of data management, Biostatistics & Programming, Data Standardization, Medical Writing, and Submissions. Innoworks is a CDISC registered solutions provider, delivering high quality clinical data while maintaining stringent regulatory compliance standards. With Innoworks as your partner, you benefit from our extensive domain knowledge, adeptness with technology, and consulting expertise to bring data driven clinical trials to a successful completion.

Our ability to provide end-to-end services is possible as we have suitable support from experts in the industry and academia. These carefully appointed partnerships have helped us deliver high quality data seamlessly.

When you select Innoworks for Clinical Data Management, you can rest assured that your clinical trial will be completed on schedule with complete and high-quality data entry. Our industry-leading unified platform technology partners and their electronic data capture (EDC) systems are applied to your needs, tailored to a decentralized/virtual trial strategy.

VISIT SOLUTIONS We provide an end-to-end Clinical Data Management solution with rapid database launch; integrated clinical data sources; expert medical coding, query management and resolution, effective external vendor data management [CRO labs/imaging], database lock ensuring quality of clean clinical trial data.

CROs that focus on data need special attention and expertise in all areas but most of it is concentrated towards proper execution and management processes & strategy for collecting the right quality, without losing trustability. We focus purely on data, ensuring a quality service is guaranteed and long-term partnerships are formed.

We then custom-design solutions that not only make data more immediately available in real time, but also faster to analyze and hence speed up decision-making — thus enabling patient safety at all times.

Whereas data-focused CROs give specialized focus, care and attention to all of these aspects on the inside (data collection processes, management process & strategy), in a well-performed service that guarantees quality — because when one confidently achieves highquality research services it encourages forging longterm partnerships.

Our Clinical Data Management team has expertise in using R which makes it possible to organize clinical data into the database with more careful vetting of the quality when compared to electronic checks from EDC system and really big SAS listings.

We validate targets according to the regulatory ruleset in order to have a submission-ready, HTA permissable target. Our team collaborate with their biostatistics department to define the core data domains/variables and generates custom tailored statistical review checks compliant with SDTM/CDISC standards.

It helps in early identification of incorrect data to reduce the possibility of errors post database lock, thus aiding development and submission packages by producing high quality statistical outputs.